<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>21(1)</volume><submitter>Simon AG</submitter><funding>Universitätsklinikum Köln</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>The prognosis of esophageal adenocarcinoma (EAC) and gastric adenocarcinoma (GAC) remains poor, and new therapeutic approaches are urgently needed. Claudin 6 (CLDN6) is an oncofetal antigen that is largely absent in healthy tissues and upregulated in several cancers, making it a promising therapeutical target. In this study, the expression of CLDN6 was assessed in an large Caucasian EAC and GAC cohort.&lt;h4>Methods&lt;/h4>RNA-Seq data from 89 EACs and 371 GACs were obtained from The Cancer Genome Atlas project and EAC/GAC cases were stratified by CLDN6 mRNA expression based on a survival-associated cutoff. For groups with CLDN6 expression above or below this cutoff, differential gene expression analyses were performed using DESeq, and dysregulated biological pathways were ide</pubmed_abstract><journal>Journal of translational medicine</journal><pagination>552</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10436499</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The tight junction protein claudin 6 is a potential target for patient-individualized treatment in esophageal and gastric adenocarcinoma and is associated with poor prognosis.</pubmed_title><pmcid>PMC10436499</pmcid><pubmed_authors>Bruns CJ</pubmed_authors><pubmed_authors>Lyu SI</pubmed_authors><pubmed_authors>Sahin U</pubmed_authors><pubmed_authors>Schroeder W</pubmed_authors><pubmed_authors>Tureci O</pubmed_authors><pubmed_authors>Simon AG</pubmed_authors><pubmed_authors>Laible M</pubmed_authors><pubmed_authors>Woll S</pubmed_authors><pubmed_authors>Fahrig L</pubmed_authors><pubmed_authors>Gebauer F</pubmed_authors><pubmed_authors>Zander T</pubmed_authors><pubmed_authors>Buettner R</pubmed_authors><pubmed_authors>Quaas A</pubmed_authors><pubmed_authors>Alakus H</pubmed_authors></additional><is_claimable>false</is_claimable><name>The tight junction protein claudin 6 is a potential target for patient-individualized treatment in esophageal and gastric adenocarcinoma and is associated with poor prognosis.</name><description>&lt;h4>Background&lt;/h4>The prognosis of esophageal adenocarcinoma (EAC) and gastric adenocarcinoma (GAC) remains poor, and new therapeutic approaches are urgently needed. Claudin 6 (CLDN6) is an oncofetal antigen that is largely absent in healthy tissues and upregulated in several cancers, making it a promising therapeutical target. In this study, the expression of CLDN6 was assessed in an large Caucasian EAC and GAC cohort.&lt;h4>Methods&lt;/h4>RNA-Seq data from 89 EACs and 371 GACs were obtained from The Cancer Genome Atlas project and EAC/GAC cases were stratified by CLDN6 mRNA expression based on a survival-associated cutoff. For groups with CLDN6 expression above or below this cutoff, differential gene expression analyses were performed using DESeq, and dysregulated biological pathways were ide</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Aug</publication><modification>2025-05-29T19:15:36.613Z</modification><creation>2024-11-05T19:25:18.718Z</creation></dates><accession>S-EPMC10436499</accession><cross_references><pubmed>37592303</pubmed><doi>10.1186/s12967-023-04433-8</doi></cross_references></HashMap>